Zachariou V, Caldarone B J, Weathers-Lowin A, George T P, Elsworth J D, Roth R H, Changeux J P, Picciotto M R
Department of Psychiatry, Yale University School of Medicine, Yale University, New Haven, CT, USA.
Neuropsychopharmacology. 2001 May;24(5):576-89. doi: 10.1016/S0893-133X(00)00224-4.
The reinforcing properties of nicotine and psychomotor stimulants are thought to be mediated through the mesolimbic dopamine (DA) system. This study investigates the role of high affinity nicotinic acetylcholine receptors (nAChRs) in cocaine place preference and examines some neurochemical changes in the mesolimbic DA system that might account for the interaction between nicotine and cocaine. 5 mg/kg is the lowest dose of cocaine able to condition a place preference in C57Bl/6 mice. Co-treatment with the nicotinic antagonist mecamylamine (1.0 mg/kg) disrupted place preference to 5 mg/kg cocaine. In addition, mice lacking the high affinity nAChR containing the beta2 subunit showed decreased place preference to 5 mg/kg cocaine, although higher doses of cocaine could condition a place preference in these knock out animals. In contrast, co-administration of a low dose of nicotine (0.2 mg/kg) potentiated place preference to a subthreshold dose of cocaine (3 mg/kg). DA turnover was monitored in several brain regions using tissue levels of DA and its primary metabolite DOPAC as an indication of DA release. Wild type mice showed decreased DA turnover following treatment with 5 mg/kg cocaine; whereas, this response was not seen in mice lacking the beta2 subunit of the nAChR. Induction of chronic fos-related antigens by cocaine was also reduced in mutant mice as compared to their wild type siblings, implying that downstream actions of cocaine were also affected by inactivation of the high affinity nAChR. These data indicate that activation of the high affinity nAChR may contribute to cocaine reinforcement.
尼古丁和精神运动兴奋剂的强化特性被认为是通过中脑边缘多巴胺(DA)系统介导的。本研究调查了高亲和力烟碱型乙酰胆碱受体(nAChRs)在可卡因位置偏爱中的作用,并研究了中脑边缘DA系统中一些可能解释尼古丁与可卡因相互作用的神经化学变化。5mg/kg是能够使C57Bl/6小鼠形成位置偏爱的最低可卡因剂量。与烟碱拮抗剂美加明(1.0mg/kg)共同给药会破坏对5mg/kg可卡因的位置偏爱。此外,缺乏含β2亚基的高亲和力nAChR的小鼠对5mg/kg可卡因的位置偏爱降低,尽管更高剂量的可卡因能使这些基因敲除动物形成位置偏爱。相反,低剂量尼古丁(0.2mg/kg)共同给药会增强对阈下剂量可卡因(3mg/kg)的位置偏爱。使用DA及其主要代谢产物DOPAC的组织水平作为DA释放的指标,监测了几个脑区的DA周转率。野生型小鼠在接受5mg/kg可卡因治疗后DA周转率降低;然而,在缺乏nAChRβ2亚基的小鼠中未观察到这种反应。与野生型同窝小鼠相比,可卡因对突变小鼠慢性fos相关抗原的诱导也减少,这意味着可卡因的下游作用也受到高亲和力nAChR失活的影响。这些数据表明高亲和力nAChR的激活可能有助于可卡因的强化作用。